Veeva etcd bla publisher

- Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.- Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions.- Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA).- Experience in Life Sciences / Pharma regulatory...

Prepare and manage BLA (Biologics License Application) submissions in e CTD format using Veeva Vault e CTD Publishing.Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions.Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA).Experience in Life Sciences / Pharma regulatory...

Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing . Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions. Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA) . Experience in Life Sciences / Pharma regulatory...

Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions.Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA).Experience in Life Sciences / Pharma regulatory...

Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions.Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA).Experience in Life Sciences / Pharma regulatory...

Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions.Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA).Experience in Life Sciences / Pharma regulatory...

We are seeking a passionate and detail-oriented Veeva eCTD BLA Publisher to support global regulatory submissions for biologics and BLA products. The ideal candidate will have hands-on experience with Veeva Vault eCTD Publishing , strong knowledge of FDA and EMA guidelines , and a proven track record of compiling, formatting, and dispatching high-quality...

- Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing. - Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions. - Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA). - Experience in Life Sciences / Pharma...

Role: Veeva CRM - TestingExperience: 5-8 yrsLocation: Pan IndiaNotice Period: Immediate to 15 daysKey ResponsibilitiesPerform functional regression and integration testing on Veeva CRM applicationsValidate workflows including approval chains content publishing and analytics trackingCollaborate with business analysts and developers to understand requirements...

Role : Veeva CRM - TestingExperience : 5-8 yrsLocation : Pan IndiaNotice Period : Immediate to 15 daysKey ResponsibilitiesPerform functional regression and integration testing on Veeva CRM applicationsValidate workflows including approval chains content publishing and analytics trackingCollaborate with business analysts and developers to understand...